Agency Information Collection Request. 30-Day Public Comment Request, 15878-15879 [2024-04613]
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15878
Federal Register / Vol. 89, No. 44 / Tuesday, March 5, 2024 / Notices
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(5) What plan for longitudinal followup of newborns identified through
newborn screening is available? For
example, will there be a patient registry
available for use by clinical providers or
by individuals/families? For how many
years would infants with the condition
be followed?
Evidence-based Review Process: The
current criteria for ACHDNC to
recommend inclusion of a condition on
the RUSP to the Secretary is based
primarily on peer-reviewed evidence
regarding the certainty that benefits of
universal screening outweigh harms
(‘‘net benefit’’). These criteria have been
largely applied to focus on the benefits
and harms to the individual child, with
much less consideration of benefits and
harms to the family, states, or to the
public health system. Financial and
opportunity costs have received less
attention by ACHDNC, in part because
of the lack of published evidence
regarding such topics.
Below is an example of what
published evidence should be
considered by the Committee when
conducting a condition evidence
review. The Committee requests
feedback regarding the example below.
When weighing certainty and net
benefit of screening for a condition, the
Committee should consider the full
range of relevant, published, peerreviewed evidence. Although such
evidence in relation to benefits and
harms to the individual child remain
paramount, the Committee should also
consider benefits and harms to the
family and to society at large, including
disproportionate impacts or disparities
related to specific conditions or
screening. For example, the Committee
could consider evidence demonstrating
benefits for the family regarding future
planning (e.g., finances, geographic
proximity to services, home design,
etc.), earlier access to early intervention
programs, or opportunity costs to the
public health system. Ideally, potential
harms and benefits should be supported
by evidence directly relevant to the
condition under review. When such
evidence is lacking, Committee
members could consider peer-reviewed
evidence from other disorders to the
extent that such evidence is considered
potentially relevant to the condition
under consideration.
Special Note to Commenters
The information obtained through this
request for information (RFI) may help
inform ACHDNC processes. Per the
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ACHDNC Charter, the Committee has
the responsibility to decide the
processes for nomination, evidence
review, and making recommendations
regarding the RUSP. How Committee
members ultimately vote on
recommending a condition for inclusion
on the RUSP will continue to reflect
their judgment on the certainty of net
benefit to the entire population of
infants born in the United States.
This RFI is issued solely for
information and planning purposes; it
does not constitute a Request for
Proposal, applications, proposal
abstracts, or quotations. This RFI does
not commit the U.S. government to
contract for any supplies or services or
make a grant or cooperative agreement
award. Further, HRSA is not seeking
proposals through this RFI and will not
accept unsolicited proposals. HRSA will
not respond to questions about the
policy issues raised in this RFI.
Responders are advised that the U.S.
government will not pay for any
information or administrative costs
incurred in response to this RFI; all
costs associated with responding to this
RFI will be solely at the interested
party’s expense.
Authority: ACHDNC is authorized by
section 1111(g) of the Public Health
Service Act, 42 U.S.C. 300b–10(g), and
the Federal Advisory Committee Act, 5
U.S.C. chapter 10.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024–04618 Filed 3–4–24; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0955–0018]
Agency Information Collection
Request. 30-Day Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be
received on or before April 4, 2024.
ADDRESSES: Written comments and
recommendations for the proposed
SUMMARY:
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information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Sherrette Funn, Sherrette.Funn@hhs.gov
or (202) 264–0041, or PRA@HHS.GOV.
When submitting comments or
requesting information, please include
the document identifier 0955–0018–30D
and project title for reference.
Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
Title of the Collection: 21st Century
Cures Act: Interoperability, Information
Blocking, and the ONC Health IT
Certification Program.
Type of Collection: Reinstatement
without change.
OMB No: 0955–0018.
Abstract: The Department of Health
and Human Services, Office of the
Secretary, Office of the National
Coordinator for Health IT Office of
Policy, is requesting an approval by
OMB for reinstatement without change
which pertains to a records and
information retention requirement
found at 45 CFR 170.402(b)(1). The
purpose and use of this records and
information retention requirement is to
verify, as necessary, health IT developer
compliance with the ONC Health IT
Certification Program (Program)
requirements, including certification
criteria and Conditions and
Maintenance of Certification.
Specifically, a health IT developer must,
for a period of 10 years beginning from
the date each of a developer’s health IT
is first certified under the Program,
retain all records and information
necessary that demonstrate initial and
ongoing compliance with the
requirements of the Program.
SUPPLEMENTARY INFORMATION:
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15879
Federal Register / Vol. 89, No. 44 / Tuesday, March 5, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN TABLE
Respondents
(if necessary)
Average
burden per
response
Total
burden
hours
Health IT Developers .......................................................................................
435
1
104
45,240
Total ..........................................................................................................
435
........................
........................
45,240
Sherrette A. Funn,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
[FR Doc. 2024–04613 Filed 3–4–24; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Stakeholder Listening Session in
Preparation for the 77th World Health
Assembly
Office of Global Affairs,
Department of Health and Human
Services.
ACTION: Notice of public listening
session; request for comments.
AGENCY:
The listening session will be
held Thursday, May 2, 2024, from 10
a.m. to 12 p.m. eastern daylight time.
This session is open to the public but
requires RSVP to oga.rsvp1@hhs.gov by
Friday, April 26, 2024. See RSVP
section in SUPPLEMENTARY INFORMATION
for details.
ADDRESSES: The session will be held
virtually. Online and dial-in
information will be shared with
registered participants.
SUPPLEMENTARY INFORMATION:
Purpose: The U.S. Department of
Health and Human Services (HHS) leads
the U.S. delegation to the 77th World
Health Assembly and will convene an
informal Stakeholder Listening Session.
The Stakeholder Listening Session is
designed to seek input from
stakeholders and subject matter experts
to help the HHS Office of Global Affairs
inform and prepare for U.S. Government
engagement at the World Health
Assembly.
The World Health Assembly is the
decision-making body of the World
Health Organization (WHO). It is
attended by delegations from all 194
WHO Member States. The main
functions of the World Health Assembly
are to determine the policies of the
Organization, appoint the DirectorGeneral, supervise financial policies,
and review and approve the proposed
program budget. The Health Assembly
is held annually in Geneva,
Switzerland. Additional information
DATES:
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Number of
responses per
respondents
Number of
respondents
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about the World Health Assembly can
be found at this website: https://
www.who.int/about/governance/worldhealth-assembly.
Matters to be Discussed: The listening
session will cover items on the
provisional agenda of the 77th World
Health Assembly. The provisional
agenda can be found at this website:
https://apps.who.int/gb/ebwha/pdf_
files/EB154/B154_39-en.pdf.
Participation is welcome from
stakeholder communities, including:
• Public health and advocacy groups
• State, local, and Tribal groups
• Private industry
• Minority health organizations
• Academic and scientific
organizations, etc.
RSVP: Persons seeking to participate
in the listening session must register by
Friday, April 26, 2024.
Registrants must include their full
name, email address, and organization,
if any, and indicate whether they are
registering as a listen-only attendee or
as a speaker participant to oga.rsvp1@
hhs.gov.
Requests to participate as a speaker
must include all of the following
information:
1. The name and email address of the
person desiring to participate
2. The organization(s) that person
represents
3. The primary agenda item(s) of
interest, listed in order of the
speaker’s priorities
Note: A separate listening session will be
held on Thursday, April 11, 2024, to discuss
the following World Health Assembly agenda
items:
• 13.2 Implementation of the
International Health Regulations
(2005)
• 13.3 Working Group on Amendments
to the International Health
Regulations (2005)
• 13.4 Intergovernmental Negotiating
Body to draft and negotiate a WHO
convention, agreement or other
international instrument on pandemic
prevention, preparedness and
response
To provide comments on these agenda
items, please see the corresponding
Federal Register notice: https://
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www.federalregister.gov/documents/
2024/02/28/2024-04080/stakeholderlistening-session-on-public-healthemergencies-preparedness-andresponse-negotiations.
Other Information: Written comments
are welcome and encouraged even if
you are attending the listening session
and should be emailed to oga.rsvp1@
hhs.gov with the subject line ‘‘Written
Comment Re: Stakeholder Listening
Session for WHA77’’ by Friday, May 3,
2023.
We look forward to your comments on
the 77th World Health Assembly.
Dated: February 28, 2024.
Susan Kim,
Principal Deputy Assistant Secretary, Office
of Global Affairs.
[FR Doc. 2024–04525 Filed 3–4–24; 8:45 am]
BILLING CODE 4150–38–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Neurological
Disorders and Stroke; Amended Notice
of Meeting
Notice is hereby given of a change in
the meeting of the National Institute of
Neurological Disorders and Stroke
Special Emphasis Panel, March 19,
2024, 9 a.m. to March 19, 2024, 6 p.m.,
National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852, which
was published in the Federal Register
on February 23, 2024, FR Doc 2024–
03818, 89 FR 14080.
This notice is being amended to
change the date of this one-day meeting
to a two-day meeting March 19, 2024, to
March 20, 2024. The meeting time
remains the same. The meeting is closed
to the public.
Dated: February 29, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–04592 Filed 3–4–24; 8:45 am]
BILLING CODE 4140–01–P
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]]>Agencies
[Federal Register Volume 89, Number 44 (Tuesday, March 5, 2024)]
[Notices]
[Pages 15878-15879]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-04613]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0955-0018]
Agency Information Collection Request. 30-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995, the Office of the Secretary (OS), Department of Health and
Human Services, is publishing the following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be received on or before April 4, 2024.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: Sherrette Funn, [email protected]
or (202) 264-0041, or [email protected]. When submitting comments or
requesting information, please include the document identifier 0955-
0018-30D and project title for reference.
SUPPLEMENTARY INFORMATION: Interested persons are invited to send
comments regarding this burden estimate or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
Title of the Collection: 21st Century Cures Act: Interoperability,
Information Blocking, and the ONC Health IT Certification Program.
Type of Collection: Reinstatement without change.
OMB No: 0955-0018.
Abstract: The Department of Health and Human Services, Office of
the Secretary, Office of the National Coordinator for Health IT Office
of Policy, is requesting an approval by OMB for reinstatement without
change which pertains to a records and information retention
requirement found at 45 CFR 170.402(b)(1). The purpose and use of this
records and information retention requirement is to verify, as
necessary, health IT developer compliance with the ONC Health IT
Certification Program (Program) requirements, including certification
criteria and Conditions and Maintenance of Certification. Specifically,
a health IT developer must, for a period of 10 years beginning from the
date each of a developer's health IT is first certified under the
Program, retain all records and information necessary that demonstrate
initial and ongoing compliance with the requirements of the Program.
[[Page 15879]]
Estimated Annualized Burden Table
----------------------------------------------------------------------------------------------------------------
Number of
Respondents (if necessary) Number of responses per Average burden Total burden
respondents respondents per response hours
----------------------------------------------------------------------------------------------------------------
Health IT Developers............................ 435 1 104 45,240
---------------------------------------------------------------
Total....................................... 435 .............. .............. 45,240
----------------------------------------------------------------------------------------------------------------
Sherrette A. Funn,
Paperwork Reduction Act Reports Clearance Officer, Office of the
Secretary.
[FR Doc. 2024-04613 Filed 3-4-24; 8:45 am]
BILLING CODE 4150-45-P
